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Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester is a chemical compound that belongs to the class of imidazo[1,5-a]pyrazine derivatives. It is a brominated ethyl ester derivative of imidazo[1,5-a]pyrazine-3-carboxylic acid, known for its versatile structure and properties. Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester is commonly used in organic synthesis as a building block for the preparation of various pharmaceutical and agrochemical compounds, making it a valuable asset in the field of organic chemistry.

1304064-99-0

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1304064-99-0 Usage

Uses

Used in Pharmaceutical Industry:
Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester is used as a key intermediate in the synthesis of pharmaceutical compounds for its ability to be readily modified and incorporated into complex molecular structures. Its unique properties allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester serves as a crucial building block in the creation of agrochemicals, such as pesticides and herbicides. Its reactivity and structural features enable the design of effective compounds targeting specific pests or weeds, thereby enhancing crop protection.
Used in Organic Synthesis:
As a versatile reactant in organic synthesis, Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester is utilized for the preparation of a wide range of chemical compounds. Its reactivity and functional groups make it suitable for various synthetic routes, leading to the formation of novel molecules with potential applications in various industries.
Used in Drug Discovery and Development:
Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester plays a significant role in drug discovery and development due to its potential to be modified and optimized for specific biological targets. Its unique structure allows for the design of compounds with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Used in Material Science:
In the field of material science, Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester can be employed in the development of new materials and technologies. Its chemical properties and reactivity make it a promising candidate for the synthesis of advanced materials with specific properties, such as improved stability, conductivity, or responsiveness to environmental stimuli.

Check Digit Verification of cas no

The CAS Registry Mumber 1304064-99-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,0,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1304064-99:
(9*1)+(8*3)+(7*0)+(6*4)+(5*0)+(4*6)+(3*4)+(2*9)+(1*9)=120
120 % 10 = 0
So 1304064-99-0 is a valid CAS Registry Number.

1304064-99-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester

1.2 Other means of identification

Product number -
Other names Imidazo[1,5-a]pyrazine-3-carboxylic acid, 1-bromo-, ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1304064-99-0 SDS

1304064-99-0Downstream Products

1304064-99-0Relevant academic research and scientific papers

Imidazopyridine CB2 agonists: Optimization of CB2/CB1 selectivity and implications for in vivo analgesic efficacy

Trotter, B. Wesley,Nanda, Kausik K.,Burgey, Christopher S.,Potteiger, Craig M.,Deng, James Z.,Green, Ahren I.,Hartnett, John C.,Kett, Nathan R.,Wu, Zhicai,Henze, Darrell A.,Penna, Kimberly Della,Desai, Reshma,Leitl, Michael D.,Lemaire, Wei,White, Rebecca B.,Yeh, Suzie,Urban, Mark O.,Kane, Stefanie A.,Hartman, George D.,Bilodeau, Mark T.

, p. 2354 - 2358 (2011)

A new series of imidazopyridine CB2 agonists is described. Structural optimization improved CB2/CB1 selectivity in this series and conferred physical properties that facilitated high in vivo exposure, both centrally and peripherally. Administration of a h

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